Update and info on Study for Ped FMS

[Guest guest]

Hi there ladies, let me start by saying that I hope April is better for

everyone.

We had our follow up this morning at Cincy Childrens with Dr Graham. He

seemed pleased with how Zoe is doing. We are doing a totally natural

program with supplements and homeopathies. There was minimal swelling and

she has improved range of motion in her knee and calf/ankle. All

measurements were equal and he told us to keep doing what we are doing.

Yeah! I know a lot of you are unsure of the path I am taking with Zoe, but

I feel that I am getting results and would much rather kill off the cause of

this than spend years treating symptoms.

On another note, while I was there, I saw a note posted at check out that

they are doing a study of kids with FMS. I did not get all the details, but

I would suppose you could call the hospital or the Rheumatology clinic to

get more info. They are looking for participants that will get care free of

charge with travel reimbursements. If you are or know anyone that might be

interested, give them a call. I do think the age for this was 11-18, but am

not positive on that.

And my last thing is to ask who will be participating in the Cincinnati

Arthritis Walk? I would love to pull a team together or join one locally if

already established.

Here is hoping that you aren't fooled tomorrow.

Joann

Zoe, 6, Pauci JRA 1 knee